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Sample GSM215002 Query DataSets for GSM215002
Status Public on Nov 19, 2007
Title Neutrophils before exercise 11
Sample type RNA
 
Source name Human netrophils before exercise
Organism Homo sapiens
Characteristics neutrophil, healthy male, age 29
before-exercise
Extracted molecule total RNA
Extraction protocol Neutrophils were isolated using OptiPrepÒ Density Gradient Medium (SIGMA). Using hematoxylin staining, we determined that this approach to neutrophil isolation consistently yielded ≥ 98% purification. Total RNA was extracted using TRIzol® reagent and purified using the RNeasy Midi columns method (Qiagen, Valencia, CA)
Label biotin
Label protocol 2 μg total RNA was used as a template for double‑stranded cDNA synthesis. Single-stranded then double-stranded cDNA was synthesized from the poly A spike-in controls, and mRNA present in the isolated total RNA using the SuperScript Double-Stranded cDNA Synthesis Kit (Invitrogen Corp., Carlsbad, CA), and a T-7-oligo(dT) primer (Integrated DNA Technologies Inc.,Coralville,IA) that contains a T7 RNA polymerase promoter site added to it’s 3' end. A portion of the resulting double-stranded cDNA was used as a template to generate biotin-tagged cRNA from an in vitro transcription reaction (IVT), using the Affymetrix GeneChip® IVT Labeling Kit.
 
Hybridization protocol 10 µg of fragmented target cRNA was hybridized at 45°C with rotation for 16 hours (Affymetrix GeneChip® Hybridization Oven 640) to probe sets present on an Affymetrix U133+2 arrays.
Scan protocol The GeneChip® arrays were washed and then stained (SAPE, streptavidin-phycoerythrin) on an Affymetrix Fluidics Station 450, followed by scanning on a GeneChip® Scanner 3000.
Description no additional
Data processing The results were quantified and analyzed using GCOS 1.4 software (Affymetrix, Inc.) using default values (Scaling Target Signal Intensity=500; Normalization, All probe sets; Parameters, all set at default values). The microarray data was analyzed using ArrayAssistÒ version 4.0.3 (STRATAGENEÒ ). We normalized the data using GC-RMA.
 
Submission date Aug 02, 2007
Last update date Aug 28, 2018
Contact name Shlomit Radom-Aizik
E-mail(s) saizik@uci.edu
Phone 949-824-2584
Organization name University of California, Irvine
Department Pediatrics
Lab Pediatric Exercise and Genomics Research Center
Street address 101 Academy
City Irvine
State/province CA
ZIP/Postal code 92617
Country USA
 
Platform ID GPL570
Series (1)
GSE8668 Effects of exercise on gene expression in human neutrophils
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE86362
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE GC-RMA

Data table
ID_REF VALUE
1007_s_at 5.8829317
1053_at 68.01551
117_at 1133.3911
121_at 9.963083
1255_g_at 4.2177362
1294_at 105.686386
1316_at 10.242624
1320_at 6.0938287
1405_i_at 3328.8706
1431_at 7.8124046
1438_at 4.4915247
1487_at 58.068485
1494_f_at 5.252711
1552256_a_at 7.4602723
1552257_a_at 49.860943
1552258_at 20.248995
1552261_at 8.043466
1552263_at 423.69183
1552264_a_at 2097.6
1552266_at 8.621864

Total number of rows: 54675

Table truncated, full table size 1087 Kbytes.




Supplementary file Size Download File type/resource
GSM215002.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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